FDA
approval
· 2023-12-21
FDA Approved: IDHIFA — Supplemental Application (Celgene Corporation)
Summary
FDA approved a supplemental application for IDHIFA (enasidenib mesylate) to expand its labeling for acute myeloid leukemia with IDH2 mutation.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for IDHIFA (ENASIDENIB MESYLATE)